ZMP
TSHZ3 (1 of 2)
Ensembl ID:
Description:
teashirt zinc finger homeobox 3 [Source:HGNC Symbol;Acc:30700]
Human Orthologue:
TSHZ3
Human Description:
teashirt zinc finger homeobox 3 [Source:HGNC Symbol;Acc:30700]
Mouse Orthologue:
Tshz3
Mouse Description:
teashirt zinc finger family member 3 Gene [Source:MGI Symbol;Acc:MGI:2442819]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7083 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40987 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34161 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15444 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7083
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032123 | Nonsense | 299 | 1066 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 48341314)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 46459425 |
GRCz11 | 7 | 46731791 |
KASP Assay ID:
554-5130.1 (used for ordering genotyping assays)
KASP Sequence:
TGGCAGCCAAGATTATCTCCTCAGCTCGTAAAAGAGCCCCTATTGAGCTA[G/T]AACTCCCCAGCTCACCAGATTCTAACGGTGGCACCCCCAAGCCTTCTTTA
Long Flanking Sequence:
GGCACCAGACAGCAGTGGCTAAGACCTTGCAGAATGTTTCACAGAACCAGAGTAGACTACTGCACCCAGCATCCGAGCCTAACCTCTTCAGTACTGTGCAGCTTTATCGGCAGAGCACCAAACTCTACGGCTCCATTTTCACTGGGGCAAGCAAATTCCGCTGCAAAGATTGCAGTGCTGCCTATGACACTCTAGTTGAGCTCACTGTGCACATGAATGAGACGGGCCACTACAGAGATGACAACCATGAGACAGACAGTGAAGGTACCAAGCGCTGGTCAAAGCCTCGCAAACGTTCCCTCCTTGAGATGGAAGGAAAGGAGGATGCCCAGAAAGTTCTCAAATGCATGTACTGTGGACATTCCTTTGAGTCACTACAGGATCTCAGTGTTCACATGATCAAAACGAAACACTACCAGAAAGTGCCTCTTAAGGAACCTGTAACTCCTGTGGCAGCCAAGATTATCTCCTCAGCTCGTAAAAGAGCCCCTATTGAGCTA[G/T]AACTCCCCAGCTCACCAGATTCTAACGGTGGCACCCCCAAGCCTTCTTTATCTGACCCCAATGACCTTCTGCAAAAGACCCCTAATCCTTACATCACACCCAATAATCGGTATGGACACCAAAACGGTGCTAGTTATGCATGGCAGTTTGAGTCGCGAAAATCCCAGATCCTGAAGTGCATGGAGTGTGGAAGCTCACATGACACATTACAGGAATTGACCGCCCATATGATGGTCACAGGACACTTCATCAAAGTCACTAACTCTGCCATCAAGAAAGGCAAACCTATCATGGAGTCAATGTCCACAACAGCTCCTAACCCCATACTTACTAATGAAGACAAGGTACAGTCAGTGCCACTTGCTGCCACTGCATTTTCCCCACCACCTCCTGCACCTCCTCCCCCTAGTATCTCTCCTGCCATCATGCCCATGGAGATTAAAAAGGAGGAGAAGGAAGTGGAGTGTACAAGAGAAACAAATAATAACAAAGACAAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40987
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032123 | Nonsense | 481 | 1066 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 48340766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 46458877 |
GRCz11 | 7 | 46731243 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCAGCAGAAAGCGAAACTGATGAGAAGTTTGAAGTTTCATCCAAGTA[T/A]CCATATTTGACAGAGGAAGATCTTGAAGAAAGCCCTAAGGGGGGGTTTGA
Long Flanking Sequence:
TTATCTGACCCCAATGACCTTCTGCAAAAGACCCCTAATCCTTACATCACACCCAATAATCGGTATGGACACCAAAACGGTGCTAGTTATGCATGGCAGTTTGAGTCGCGAAAATCCCAGATCCTGAAGTGCATGGAGTGTGGAAGCTCACATGACACATTACAGGAATTGACCGCCCATATGATGGTCACAGGACACTTCATCAAAGTCACTAACTCTGCCATCAAGAAAGGCAAACCTATCATGGAGTCAATGTCCACAACAGCTCCTAACCCCATACTTACTAATGAAGACAAGGTACAGTCAGTGCCACTTGCTGCCACTGCATTTTCCCCACCACCTCCTGCACCTCCTCCCCCTAGTATCTCTCCTGCCATCATGCCCATGGAGATTAAAAAGGAGGAGAAGGAAGTGGAGTGTACAAGAGAAACAAATAATAACAAAGACAAGAAAGCAGCAGAAAGCGAAACTGATGAGAAGTTTGAAGTTTCATCCAAGTA[T/A]CCATATTTGACAGAGGAAGATCTTGAAGAAAGCCCTAAGGGGGGGTTTGACATTTTGAAGTCTCTTGAGAATACAGTAACATCTGCCATCAACAAAGCACAGAATGGCACACCCAGCTGGGGAGGCTATCCCAGTATCCACGCTGCCTACCAGCTTCCAAACATTATGAAACTCTCCCTGCGCAACTCAGGGAAAAGTTCTCCTCTGAAGTATATGTTTTCTGGAGAAGAGCTCCTGTCTCCTACCAAAAGCCAACCTCTAATTTCACCACCTAGTTGCCAAACATCCCCTTTACCCAAAAACAACTTTCATGCCATGGAGGAGCTGGTCAAAAAAGTCACAGAAAAAGTGGCCAAAGTAGAGGAGAAAATGAGGGATCCTGGAGCAAGGTCTTCCCCTCTGAGACGGACCACACCCTCTCCATGCAGTAGTGATGCAGGGGAATCTGCCAGAGGGGAGTCCCCTAAGGAAAGAAGAGGAGCCAAAACCCCTGAGACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34161
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032123 | Nonsense | 920 | 1066 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 48339450)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 46457561 |
GRCz11 | 7 | 46729927 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCAAGTACATTATGTCAGACCTCAGTCCACAGGAGCGCATGCATATTT[C/A]GCGCTTTACTGGACTCTCAATGACGACCATTAGCCACTGGCTAGCAAATG
Long Flanking Sequence:
GACGAATGACCATCTAGACCGCTACTTCTACCACATCAACAATGACCAGCCTATTGATCTGACCAAAGGCAAGAGCGATAAGAGCAACTCTTTAGGATCTGCTGCCCTGTCCTCCTCCACCTCCACACCCACTTCAATTTCACCGTCATCAACCATCACCATGGCCAAAGCCTCATCCGCTGTGGCTTCCTTCATGTCTAACTCACCTTTGCGTGAAAATGCCCTGTCTGACATCTCCGACATGCTACGTAACCTCACAGAAAACCATGCATCTAAGTCCTCCACTCCAACAAGTCTGTCAGAGCGATCAGACATAGATGGATCTACACCTGAGGAATCAGAGGAGATCTCTCCTGCTCAGAAACGAAAAGGCAGACAGTCCAATTGGAATCCTCAGCATTTGCTCATTCTGCAGGCACAATTTGCCTCCAGTTTGCGGCAAACAGGGGACGGCAAGTACATTATGTCAGACCTCAGTCCACAGGAGCGCATGCATATTT[C/A]GCGCTTTACTGGACTCTCAATGACGACCATTAGCCACTGGCTAGCAAATGTCAAATACCAGCTGAGGCGGACAGGTGGCACAAAATTCTTGAAAAATCTAGACTCTGGCCACCCTGTCTTCTTCTGCAGTGACTGTGCATCACAGATTCGTTCCCCCTCTACCTACGTCAGCCATCTTGAGTCACATTTGGGCTTTCGGCTCAGGGACCTGGCTAAGTTGTCTGGAGAACATCTTGTTAGCCAGATCTCTCGCCACACCAAGGGACTATCTGAGAAACTGCTTTCAGCCCAAGCGCATTCTTTGGCTCATACGATCGCGAACCCAAGTCCTCACTCACTTTCCCCCTCCCCTTCCCCAGATGAGGAGGCAAATGGCACCTCGTATCAGTGTAAACTGTGTAATCGGACTTTTGCCAGCAAACACGCCGTCAAGCTCCATCTGAGTAAGACCCATGGTAAATCTCCAGAGGACCATCTTATGTATGTTAGTGAACTTGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15444
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000032123 | Nonsense | 1028 | 1066 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 7 (position 48339059)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 46457170 |
GRCz11 | 7 | 46729536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCCCTCCCCTTCCCCAGATGWGGAGGCAAATGGCACCTCRTATCAGTG[T/A]AAACTGTGTAATCGGACTTTTGCCAGCAAACACGCCGTCAAGCTCCATCT
Long Flanking Sequence:
CCTCAGCATTTGCTCATTCTGCAGGCACAATTTGCCTCCAGTTTGCGGCAAACAGGGGACGGCAAGTACATTATGTCAGACCTCAGTCCACAGGAGCGCATGCATATTTCGCGCTTTACTGGACTCTCAATGACGACCATTAGCCACTGGCTAGCAAATGTCAAATACCAGCTGAGGCGGACAGGTGGCACAAAATTCTTGAAAAATCTAGACTCTGGCCACCCTGTCTTCTTCTGCAGTGACTGTGCATCACAGATTCGTTCCCCCTCTACCTACGTCAGCCATCTTGAGTCACATTTGGGCTTTCGGCTCAGGGACCTGGCTAAGTTGTCTGGAGAACATCTTGTTAGCCAGATCTCTCGCCACACCAAGGGACTATCTGAGAAACTGCTTTCAGCCCAAGCGCATTCTTTGGCTCATACGATCGCGAACCCAAGTCCTCACTCACTTTCCCCCTCCCCTTCCCCAGATGAGGAGGCAAATGGCACCTCGTATCAGTG[T/A]AAACTGTGTAATCGGACTTTTGCCAGCAAACACGCCGTCAAGCTCCATCTGAGTAAGACCCATGGTAAATCTCCAGAGGACCATCTTATGTATGTTAGTGAACTTGAGAAACCTTAGCGATGGCCAAGGACAAAAACTCTCTTATCTCTTTATCTCCTGTCCTTTTTTCAAGCCTTCTGACTAACATTTCTTAAGGAAAAAAAAGAACTGAAAGTAATTAACAAAGAACTAACTGCACATAGATGCCAGAAAACTACTGTTTAGTTTTGGCACATAATTTGGAGTTTTATTTTCCTCTGGGGAACATTCATTTGGCTCTAGAGACGTTCATTTTCTGCATTTTCAGTTTACAATGGAAAACAGAGAAAATGATGGCAAATGATAATTTTCTAACTGTGCAGTGAAGAGGTCACTGGTAAAATATGAAGGTAAATAAAAAAGACAAAATGAAGTTGTATGTATTTGAAAGTTGTGTAAATTGAGTTTTTTTGGCATCCTTG
Associated Phenotype:
Not determined